Linked mercury methylation and nitrification across oxic subpolar regions

Marissa C. Despins, R. Mason, A. Aguilar‐Islas, C. Lamborg, C. R. Hammerschmidt, Silvia E. Newell
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Abstract

Methylmercury (MeHg) is a neurotoxin that bioaccumulates to potentially harmful concentrations in Arctic and Subarctic marine predators and those that consume them. Monitoring and modeling MeHg bioaccumulation and biogeochemical cycling in the ocean requires an understanding of the mechanisms behind net mercury (Hg) methylation. The key functional gene pair for Hg methylation, hgcAB, is widely distributed throughout ocean basins and spans multiple microbial phyla. While multiple microbially mediated anaerobic pathways for Hg methylation in the ocean are known, the majority of hgcA homologs have been found in oxic subsurface waters, in contrast to other ecosystems. In particular, microaerophilic Nitrospina, a genera of nitrite-oxidizing bacteria containing a hgcA-like sequence, have been proposed as a potentially important Hg methylator in the upper ocean. The objective of this work was therefore to examine the potential of nitrifiers as Hg methylators and quantify total Hg and MeHg across three Arctic and Subarctic seas (the Gulf of Alaska, the Bering Sea and the Chukchi Sea) in regions where Nitrospina are likely present. In Spring 2021, samples for Hg analysis were obtained with a trace metal clean rosette across these seas. Mercury methylation rates were quantified in concert with nitrification rates using onboard incubation experiments with additions of stable isotope-labeled Hg and NH4 +. A significant correlation between Hg methylation and nitrification was observed across all sites (R 2 = 0.34, p < 0.05), with the strongest correlation in the Chukchi Sea (R 2 = 0.99, p < 0.001). Nitrospina-specific hgcA-like genes were detected at all sites. This study, linking Hg methylation and nitrification in oxic seawater, furthers understanding of MeHg cycling in these high latitude waters, and the ocean in general. Furthermore, these studies inform predictions of how climate and human interactions could influence MeHg concentrations across the Arctic in the future.
跨缺氧亚极区汞甲基化和硝化作用的关联
甲基汞(MeHg)是一种神经毒素,在北极和亚北极海洋捕食者和食用它们的动物体内生物积累到可能有害的浓度。监测和模拟海洋中甲基汞的生物积累和生物地球化学循环需要了解净汞甲基化背后的机制。Hg甲基化的关键功能基因对hgcAB广泛分布在海洋盆地中,跨越多个微生物门。虽然已知海洋中汞甲基化的多种微生物介导的厌氧途径,但与其他生态系统相比,大多数hgcA同源物已在含氧地下水中被发现。特别是,微嗜气硝化菌(Nitrospina)是一种亚硝酸盐氧化细菌,含有类似hgca的序列,被认为是上层海洋中潜在的重要汞甲基化物。因此,这项工作的目的是研究硝化菌作为汞甲基化剂的潜力,并量化三个北极和亚北极海域(阿拉斯加湾、白令海和楚科奇海)中可能存在亚硝基刺虫的地区的汞和甲基汞总量。2021年春季,在这些海洋中获得了痕量金属清洁花环的汞分析样本。通过添加稳定同位素标记的Hg和NH4 +的机载孵育实验,量化了汞甲基化率和硝化率。汞甲基化与硝化之间存在显著相关性(r2 = 0.34, p < 0.05),其中楚科奇海的相关性最强(r2 = 0.99, p < 0.001)。所有位点均检测到硝基spina特异性hgca样基因。本研究将含氧海水中的汞甲基化和硝化作用联系起来,进一步了解这些高纬度水域和海洋中的甲基汞循环。此外,这些研究为预测未来气候和人类相互作用如何影响整个北极地区的甲基汞浓度提供了信息。
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